International audienceFrom 2000, our two research groups independently and simultaneously designed and developed a novel family of electrophilic fluorinating reagents based on the use of Cinchona alkaloids. The chiral N-fluoro ammonium salts demonstrated the highest efficiency compared to prior art in enantioselective electrophilic fluorination for a wide range of substrates. In this account, we tell our respective stories, how the same idea germinated in our laboratories, the characterization of the chiral reagents, the use in stoichiometric quantity then the development of a catalytic version, the application to the synthesis of chiral fluorinated molecules of pharmaceutical interest, and finally the exploitation of our reagents by other ...
The introduction of fluorine atoms into organic molecules significantly changes their physical, chem...
The first enantioselective route to both enantiomers of <i>cis</i>-1-Boc-3-fluoropiperidin-4-ol, a h...
This work is concerned with the development of the synthesis of a series of N-anthracenyl cinchona s...
International audienceFrom 2000, our two research groups independently and simultaneously designed a...
The introduction of fluorine into molecules is an important tool in the agrochemical and pharmaceuti...
The chemistry of bioactive organofluorine compounds is a rapidly developing area of research because...
The enantioselective electrophilic fluorination of α-aryl-tetralones is promoted by cinchonine/selec...
The demand for chiral synthetic compounds has led the field of asymmetric catalysis to discover, exp...
The diastereoisomers 8-fluoroquininone and 8-fluoroquinidinone were synthesised, separated and their...
International audienceThis personal account summarizes our contribution to the ion pairing organocat...
In this thesis, the synthesis, reactivity and enantioselectivity of novel chiral Selectfluor Analogu...
Enantioenriched fluorinated heterocycles can be prepared through fluorocyclizations of prochiral ind...
Enantiopure N-fluorocinchona alkaloids promoted the electrophilic fluorodesilylation of allyl silane...
THESIS 10151Over the past three decades, the synthesis of enantiomerically pure products became a ma...
Conspectus The vicinal fluorofunctionalization of alkenes is an attractive transformation that conve...
The introduction of fluorine atoms into organic molecules significantly changes their physical, chem...
The first enantioselective route to both enantiomers of <i>cis</i>-1-Boc-3-fluoropiperidin-4-ol, a h...
This work is concerned with the development of the synthesis of a series of N-anthracenyl cinchona s...
International audienceFrom 2000, our two research groups independently and simultaneously designed a...
The introduction of fluorine into molecules is an important tool in the agrochemical and pharmaceuti...
The chemistry of bioactive organofluorine compounds is a rapidly developing area of research because...
The enantioselective electrophilic fluorination of α-aryl-tetralones is promoted by cinchonine/selec...
The demand for chiral synthetic compounds has led the field of asymmetric catalysis to discover, exp...
The diastereoisomers 8-fluoroquininone and 8-fluoroquinidinone were synthesised, separated and their...
International audienceThis personal account summarizes our contribution to the ion pairing organocat...
In this thesis, the synthesis, reactivity and enantioselectivity of novel chiral Selectfluor Analogu...
Enantioenriched fluorinated heterocycles can be prepared through fluorocyclizations of prochiral ind...
Enantiopure N-fluorocinchona alkaloids promoted the electrophilic fluorodesilylation of allyl silane...
THESIS 10151Over the past three decades, the synthesis of enantiomerically pure products became a ma...
Conspectus The vicinal fluorofunctionalization of alkenes is an attractive transformation that conve...
The introduction of fluorine atoms into organic molecules significantly changes their physical, chem...
The first enantioselective route to both enantiomers of <i>cis</i>-1-Boc-3-fluoropiperidin-4-ol, a h...
This work is concerned with the development of the synthesis of a series of N-anthracenyl cinchona s...